Kobayashi Masao, Satomi Hidetoshi, Chikaraishi Hisaya, Samejima Hironobu, Horiguchi Julian, Kanzaki Ryu, Maniwa Tomohiro, Honma Keiichiro, Okami Jiro
Department of General Thoracic Surgery, Osaka International Cancer Institute, 3-1-69, Otemae, Chuo-Ku, Osaka, Osaka, 540-0008, Japan.
Department of Pathology, Osaka International Cancer Institute, 3-1-69, Otemae, Chuo-Ku, Osaka, Osaka, 540-0008, Japan.
Surg Case Rep. 2024 Oct 28;10(1):248. doi: 10.1186/s40792-024-02043-0.
Pulmonary nodules in patients with soft tissue sarcomas are likely pulmonary metastases, whereas synchronous primary pulmonary sarcomas are rare. Without surgery, determining whether a solitary pulmonary nodule is a primary or metastatic nodule is difficult. Herein, we report a rare case of a primary pulmonary sarcoma that presented synchronously with a primary dedifferentiated liposarcoma.
A 77-year-old man presented to another hospital with left inguinal swelling and a suspected recurrent inguinal hernia. Computed tomography revealed a left inguinal mass and pure-solid nodule in the left lung and the patient was referred to our hospital for detailed examination and treatment. The inguinal mass was pathologically diagnosed as a dedifferentiated liposarcoma using needle biopsy, whereas bronchoscopic biopsy revealed histological findings suggestive of a sarcoma; however, the primary site could not be determined. Positron emission tomography-computed tomography revealed no high-accumulation lesions except for the two sarcomas. We decided to perform surgery on both sarcomas for diagnostic and curative purposes. The surgical specimens showed that the two sarcomas were different. Based on the immunohistochemical staining findings of MDM2, a left inguinal dedifferentiated liposarcoma and primary pulmonary unclassified sarcoma were diagnosed. The patient displayed no evidence of recurrence 1 year after surgery.
We encountered a rare case of synchronous multiple primary sarcomas, one presenting in the lung and the other in the soft tissue. Surgery was required to achieve a definitive diagnosis for the patient, who achieved disease-free survival at 1 year. This case suggests that proactive resection of pulmonary nodules in patients with soft tissue sarcomas may be feasible as a diagnostic treatment if complete resection is achieved.
软组织肉瘤患者的肺结节很可能是肺转移瘤,而同期发生的原发性肺肉瘤则很罕见。在未进行手术的情况下,很难确定孤立性肺结节是原发性还是转移性结节。在此,我们报告一例罕见的原发性肺肉瘤病例,该病例与原发性去分化脂肪肉瘤同期出现。
一名77岁男性因左腹股沟肿胀及疑似复发性腹股沟疝就诊于另一家医院。计算机断层扫描显示左腹股沟有肿块,左肺有纯实性结节,患者被转诊至我院进行详细检查和治疗。经针吸活检,腹股沟肿块病理诊断为去分化脂肪肉瘤,而支气管镜活检显示组织学结果提示为肉瘤;然而,无法确定原发部位。正电子发射断层扫描-计算机断层扫描显示除这两个肉瘤外无高聚集性病变。为了诊断和治疗,我们决定对这两个肉瘤都进行手术。手术标本显示这两个肉瘤不同。根据MDM2的免疫组化染色结果,诊断为左腹股沟去分化脂肪肉瘤和原发性肺未分类肉瘤。术后1年,患者未出现复发迹象。
我们遇到一例罕见的同期多发原发性肉瘤病例,一个发生在肺部,另一个发生在软组织。需要通过手术才能对患者做出明确诊断,该患者术后1年实现了无病生存。该病例表明,如果能实现完全切除,对软组织肉瘤患者的肺结节进行积极切除作为诊断性治疗可能是可行的。